関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Iodoacetic Acid | HCID 5240 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Tert-butyl [5-(methoxymethyl)-1,3,4-thiadiazol-2-yl]carbamate | HCID 84382575 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | {2-[(tert-butoxycarbonyl)imino]-5-(methoxymethyl)-1,3,4-thiadiazol-3(2H)-yl}acetic acid | HCID 67116892 | 89.8% |
反応手順
Iodoacetic acid (409.3 g, 2.2 mol, 1.5 eq) is added in one portion to a solution of tert-butyl [5-(methoxymethyl)-1,3,4-thiadiazol-2-yl]carbamate a31 (360 g, 1.468 mol, 1 eq) in tetrahydrofurane (3 l) at room temperature. Sodium hydride (52.83 g, 2.2 mol, 1.5 eq) is then added portionwise, in 30 minutes, at room temperature. The reaction mixture is heated at 60° C. for the night, and the solvent is evaporated under reduced pressure. Water is added to the residue, the solution is acidified to pH=2 with aqueous 6N HCl, then extracted with CH2Cl2. The organic layer is washed with 10% aqueous Na2S2O3 (to remove the coloration of iodine) and evaporated to dryness to furnish 455.7 g of {2-[(tert-butoxycarbonyl)imino]-5-(methoxymethyl)-1,3,4-thiadiazol-3(2H)-yl}acetic acid a33 which is used directly in the next step without any further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08822508B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-0f53db14562843d99ed393f961dd7ad2 |
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| 出典メモ | uspto-grants-2014_09 |
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