Isobutyl chloroformate → 6-(Hydroxymethyl)-2H-benzo[b][1,4]thiazin-3(4H)-one
Reaction equation
[O:1]=[C:2]1[NH:7][C:6]2[CH:8]=[C:9]([C:12](O)=[O:13])[CH:10]=[CH:11][C:5]=2[S:4][CH2:3]1.C(OC(Cl)=O)C(C)C>O1CCCC1.C(N(CC)CC)C>[OH:13][CH2:12][C:9]1[CH:10]=[CH:11][C:5]2[S:4][CH2:3][C:2](=[O:1])[NH:7][C:6]=2[CH:8]=1Participants
5
Conditions
- Temperature
- 0 °C
Procedure
The acid (a) in tetrahydrofuran (50 ml) and triethylamine (4.7 ml) was cooled to 0° C. and isobutylchloroformate (4.02 ml) was added dropwise and the solution was stirred at 0° C. for 2 hours, when it was filtered into a stirred solution of sodium borohydride (3.14 g) in ice/water (50 ml). The mixture was stirred at 0° C. for 1 hour and allowed to warm to room temperature. It was acidified with 2M hydrochloric acid, evaporated to half volume, and the resulting product was collected, washed with water and dried in vacuo, to give a white solid (4.5 g).
Workup
- filtrationwhen it was filtered into a stirred solution of sodium borohydride (3.14 g) in ice/water (50 ml)
- stirringThe mixture was stirred at 0° C. for 1 hour
- temperatureto warm to room temperature
- customevaporated to half volume
- customthe resulting product was collected
- washwashed with water
- customdried in vacuo
Sources & evidence
- ORD record
- ord-2cb42db0964a4396b4e33e701f452adb
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07622481B2
Reaction notes
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