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1-Chloro-2-pentyne → (2S,3R,6S)-2,6-Dimethyl-4-(4-pent-2-ynyloxy-benzenesulfonyl)-morpholine-3-carboxylic acid methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-Chloro-2-pentyne | HCID 89764 | — |
| 反応物 | (2S,3R,6S)-4-(4-Hydroxy-benzenesulfonyl)-2,6-dimethyl-morpholine-3-carboxylic acid methyl ester | HCID 12016690 | — |
| 生成物 | (2S,3R,6S)-2,6-Dimethyl-4-(4-pent-2-ynyloxy-benzenesulfonyl)-morpholine-3-carboxylic acid methyl ester | HCID 12016687 | — |
反応手順
The title compound was prepared in a manner similar to Preparation 3 from 1-chloro-pent-2-yne and (2S,3R,6S)-4-(4-Hydroxy-benzenesulfonyl)-2,6-dimethyl-morpholine-3-carboxylic acid methyl ester. 1HNMR (400 MHz, CDCl3): δ=7.70 (d, J=8.9 Hz, 2H), 7.0 (d, J=8.9 Hz, 2H), 4.71 (bs, 2H), 4.52 (q, J=7.0 Hz, 1H), 4.27 (s, 1H), 3.97 (m, 1H), 3.54 (s, 3H), 2.98 (dd, J=12.1 and 10.8, 1H), 2.21 (m, 2H), 1.44 (d, J=6.9 Hz, 3H), 1.11 (t, J=7.5 Hz, 3H), 1.05 (d, J=6.0 Hz, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06387901B1 |
| 出典データセット | uspto-grants-2002_05 |
| ORD ID | ord-adc9652276bf4a8c9b7e73dee505412c |
| 出典メモ | uspto-grants-2002_05 |