Hydrochloric Acid → HCID 66706657, compound

HRID 2041386Notes

Reaction equation

HRID 2041386 reaction equation
C(OC([N:8]1[CH2:14][CH2:13][C:12]2[C:15]([S:20][C:21](=O)N(C)C)=[C:16]([Cl:19])[CH:17]=[CH:18][C:11]=2[CH2:10][CH2:9]1)=O)(C)(C)C.Br.BrC[C:29]1[CH:34]=[CH:33][N:32]=[CH:31][CH:30]=1.Cl>>[ClH:19].[Cl:19][C:16]1[CH:17]=[CH:18][C:11]2[CH2:10][CH2:9][NH:8][CH2:14][CH2:13][C:12]=2[C:15]=1[S:20][CH2:21][C:29]1[CH:34]=[CH:33][N:32]=[CH:31][CH:30]=1

Participants

4

Reactant 3

HCID 313Hydrochloric AcidHCID 127522194-(Bromomethyl)pyridine hbrHCID 576559793-tert-butoxycarbonyl-7-chloro-6-dimethylaminocarbonylthio-2,3,4,5-tetrahydro-1H-benzo[d]azepine

Product 1

HCID 66706657HCID 66706657, compound

Procedure

Use a method similar to the Example 387, using 3-tert-butoxycarbonyl-7-chloro-6-dimethylcarbamoylthio-2,3,4,5-tetrahydro-1H-benzo[d]azepine and 4-bromomethylpyridine hydrobromide to give, after hydrochloride formation by the General Procedure 2-2, the title compound as a white solid. MS (APCI+) m/z: 305 (M+H)+.

Workup

  1. customto give

Sources & evidence

ORD record
ord-46a9100a684d4d21806c247d22cba1d6
Source dataset
uspto-grants-2013_11
Patent number
US08580780B2

Reaction notes

Loading…